53 results on '"Baldwin ME"'
Search Results
2. Notes from the Field Preface Spring 2023
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Baldwin Mei and Kaori Yamamoto
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Theory and practice of education ,LB5-3640 ,Mathematics ,QA1-939 - Abstract
Developing and Supporting Teachers' Mathematical Pedagogy
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- 2023
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3. Preface Fall 2022
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Davidson Barr and Baldwin Mei
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Theory and practice of education ,LB5-3640 ,Mathematics ,QA1-939 - Published
- 2022
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4. Perspectives on the Evolution of MathChavrusa from Pre-COVID to Now
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Baldwin Mei, Mine Cekin, and Rochy Flint
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Theory and practice of education ,LB5-3640 ,Mathematics ,QA1-939 - Abstract
Improving Discourse in Mathematics Education
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- 2022
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5. Notes from the Field Preface Fall 2022
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Davidson Barr and Baldwin Mei
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Theory and practice of education ,LB5-3640 ,Mathematics ,QA1-939 - Abstract
Improving Discourse in Mathematics Education
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- 2022
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6. Endovascular or open surgical management for inadvertent cannulation of vertebral artery during central venous cannulation?
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RPS. Gambhir, M Garg, O Hargrove, Baldwin Melissa, and N Kandasamy
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Diseases of the circulatory (Cardiovascular) system ,RC666-701 ,Surgery ,RD1-811 - Abstract
Inadvertent cannulation of vertebral artery while attempting to insert a central venous cannula in the internal jugular vein is a very rare complication and can occur inspite of use of ultrasound guidance. This case report discusses the management of vertebral artery cannulation in a 56 year old lady electively admitted for hepatectomy. Once recognised, rather than catheter removal and external compression which can be fatal, an immediate multidisciplinary discussion must make the choice between endovascular intervention or open repair, each intervention carries its risks. In our case it was managed successfully by open surgical approach.
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- 2022
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7. Economic Benefits of Reliable Nondestructive Evaluation Standards
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Doherty, JE, primary, Baldwin, ME, additional, and LaGrotta, JM, additional
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8. Plasmin activates the lymphangiogenic growth factors VEGF-C and VEGF-D
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McColl, BK, Baldwin, ME, Roufail, S, Freeman, C, Moritz, RL, Simpson, RJ, Alitalo, K, Stacker, SA, Achen, MG, McColl, BK, Baldwin, ME, Roufail, S, Freeman, C, Moritz, RL, Simpson, RJ, Alitalo, K, Stacker, SA, and Achen, MG
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Vascular endothelial growth factor (VEGF) C and VEGF-D stimulate lymphangiogenesis and angiogenesis in tissues and tumors by activating the endothelial cell surface receptor tyrosine kinases VEGF receptor (VEGFR) 2 and VEGFR-3. These growth factors are secreted as full-length inactive forms consisting of NH2- and COOH-terminal propeptides and a central VEGF homology domain (VHD) containing receptor binding sites. Proteolytic cleavage removes the propeptides to generate mature forms, consisting of dimers of the VEGF homology domain, that bind receptors with much greater affinity than the full-length forms. Therefore, proteolytic processing activates VEGF-C and VEGF-D, although the proteases involved were unknown. Here, we report that the serine protease plasmin cleaved both propeptides from the VEGF homology domain of human VEGF-D and thereby generated a mature form exhibiting greatly enhanced binding and cross-linking of VEGFR-2 and VEGFR-3 in comparison to full-length material. Plasmin also activated VEGF-C. As lymphangiogenic growth factors promote the metastatic spread of cancer via the lymphatics, the proteolytic activation of these molecules represents a potential target for antimetastatic agents. Identification of an enzyme that activates the lymphangiogenic growth factors will facilitate development of inhibitors of metastasis.
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- 2003
9. HUMAN HERPESVIRUSES AND TEMPORAL ARTERITIS
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Clayton A. Wiley, Baldwin Me, and Hamilton Rl
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Cellular and Molecular Neuroscience ,Pathology ,medicine.medical_specialty ,Neurology ,business.industry ,medicine ,Neurology (clinical) ,General Medicine ,Arteritis ,medicine.disease ,business ,Pathology and Forensic Medicine - Published
- 1996
10. RASSF1C modulates the expression of a stem cell renewal gene, PIWIL1
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Reeves Mark E, Baldwin Melissa L, Aragon Robert, Baldwin Scott, Chen Shin-Tai, Li Xinmin, Mohan Subburaman, and Amaar Yousef G
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RASSF1C ,PIWIL1 ,Gene expression ,RASSF1C target genes ,ERK1/2 ,Medicine ,Biology (General) ,QH301-705.5 ,Science (General) ,Q1-390 - Abstract
Abstract Background RASSF1A and RASSF1C are two major isoforms encoded by the Ras association domain family 1 (RASSF1) gene through alternative promoter selection and mRNA splicing. RASSF1A is a well established tumor suppressor gene. Unlike RASSF1A, RASSF1C appears to have growth promoting actions in lung cancer. In this article, we report on the identification of novel RASSF1C target genes in non small cell lung cancer (NSCLC). Methods Over-expression and siRNA techniques were used to alter RASSF1C expression in human lung cancer cells, and Affymetrix-microarray study was conducted using NCI-H1299 cells over-expressing RASSF1C to identify RASSF1C target genes. Results The microarray study intriguingly shows that RASSF1C modulates the expression of a number of genes that are involved in cancer development, cell growth and proliferation, cell death, and cell cycle. We have validated the expression of some target genes using qRT-PCR. We demonstrate that RASSF1C over-expression increases, and silencing of RASSF1C decreases, the expression of PIWIL1 gene in NSCLC cells using qRT-PCR, immunostaining, and Western blot analysis. We also show that RASSF1C over-expression induces phosphorylation of ERK1/2 in lung cancer cells, and inhibition of the MEK-ERK1/2 pathway suppresses the expression of PIWIL1 gene expression, suggesting that RASSF1C may exert its activities on some target genes such as PIWIL1 through the activation of the MEK-ERK1/2 pathway. Also, PIWIL1 expression is elevated in lung cancer cell lines compared to normal lung epithelial cells. Conclusions Taken together, our findings provide significant data to propose a model for investigating the role of RASSF1C/PIWIL1 proteins in initiation and progression of lung cancer.
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- 2012
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11. Ras-association domain family 1C protein promotes breast cancer cell migration and attenuates apoptosis
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Aragon Robert J, Moretz Jeremy M, Chen Shin-Tai, Baldwin Melissa L, Baldwin Scott W, Reeves Mark E, Li Xinmin, Strong Donna D, Mohan Subburaman, and Amaar Yousef G
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Abstract Background The Ras association domain family 1 (RASSF1) gene is a Ras effector encoding two major mRNA forms, RASSF1A and RASSF1C, derived by alternative promoter selection and alternative mRNA splicing. RASSF1A is a tumor suppressor gene. However, very little is known about the function of RASSF1C both in normal and transformed cells. Methods Gene silencing and over-expression techniques were used to modulate RASSF1C expression in human breast cancer cells. Affymetrix-microarray analysis was performed using T47D cells over-expressing RASSF1C to identify RASSF1C target genes. RT-PCR and western blot techniques were used to validate target gene expression. Cell invasion and apoptosis assays were also performed. Results In this article, we report the effects of altering RASSF1C expression in human breast cancer cells. We found that silencing RASSF1C mRNA in breast cancer cell lines (MDA-MB231 and T47D) caused a small but significant decrease in cell proliferation. Conversely, inducible over-expression of RASSF1C in breast cancer cells (MDA-MB231 and T47D) resulted in a small increase in cell proliferation. We also report on the identification of novel RASSF1C target genes. RASSF1C down-regulates several pro-apoptotic and tumor suppressor genes and up-regulates several growth promoting genes in breast cancer cells. We further show that down-regulation of caspase 3 via overexpression of RASSF1C reduces breast cancer cells' sensitivity to the apoptosis inducing agent, etoposide. Furthermore, we found that RASSF1C over-expression enhances T47D cell invasion/migration in vitro. Conclusion Together, our findings suggest that RASSF1C, unlike RASSF1A, is not a tumor suppressor, but instead may play a role in stimulating metastasis and survival in breast cancer cells.
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- 2010
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12. Vascular Endothelial Growth Factor C and D Signaling Pathways as Potential Targets for the Treatment of Neovascular Age-Related Macular Degeneration: A Narrative Review.
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Leitch IM, Gerometta M, Eichenbaum D, Finger RP, Steinle NC, and Baldwin ME
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The development of treatments targeting the vascular endothelial growth factor (VEGF) signaling pathways have traditionally been firstly investigated in oncology and then advanced into retinal disease indications. Members of the VEGF family of endogenous ligands and their respective receptors play a central role in vasculogenesis and angiogenesis during both development and physiological homeostasis. They can also play a pathogenic role in cancer and retinal diseases. Therapeutic approaches have mostly focused on targeting VEGF-A signaling; however, research has shown that VEGF-C and VEGF-D signaling pathways are also important to the disease pathogenesis of tumors and retinal diseases. This review highlights the important therapeutic advances and the remaining unmet need for improved therapies targeting additional mechanisms beyond VEGF-A. Additionally, it provides an overview of alternative VEGF-C and VEGF-D signaling involvement in both health and disease, highlighting their key contributions in the multifactorial pathophysiology of retinal disease including neovascular age-related macular degeneration (nAMD). Strategies for targeting VEGF-C/-D signaling pathways will also be reviewed, with an emphasis on agents currently being developed for the treatment of nAMD., (© 2024. The Author(s).)
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- 2024
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13. Duration of cardiopulmonary resuscitation and phenotype of post-cardiac arrest brain injury.
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Coppler PJ, Elmer J, Doshi AA, Guyette FX, Okubo M, Ratay C, Frisch AN, Steinberg A, Weissman A, Arias V, Drumheller BC, Flickinger KL, Faro J, Schmidhofer M, Rhinehart ZJ, Hansra BS, Fong-Isariyawongse J, Barot N, Baldwin ME, Murat Kaynar A, Darby JM, Shutter LA, Mettenburg J, and Callaway CW
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- Humans, Cohort Studies, Coma complications, Cardiopulmonary Resuscitation adverse effects, Cardiopulmonary Resuscitation methods, Brain Edema etiology, Heart Arrest complications, Hypoxia-Ischemia, Brain etiology, Brain Injuries complications, Out-of-Hospital Cardiac Arrest therapy
- Abstract
Background: Patients resuscitated from cardiac arrest have variable severity of primary hypoxic ischemic brain injury (HIBI). Signatures of primary HIBI on brain imaging and electroencephalography (EEG) include diffuse cerebral edema and burst suppression with identical bursts (BSIB). We hypothesize distinct phenotypes of primary HIBI are associated with increasing cardiopulmonary resuscitation (CPR) duration., Methods: We identified from our prospective registry of both in-and out-of-hospital CA patients treated between January 2010 to January 2020 for this cohort study. We abstracted CPR duration, neurological examination, initial brain computed tomography gray to white ratio (GWR), and initial EEG pattern. We considered four phenotypes on presentation: awake; comatose with neither BSIB nor cerebral edema (non-malignant coma); BSIB; and cerebral edema (GWR ≤ 1.20). BSIB and cerebral edema were considered as non-mutually exclusive outcomes. We generated predicted probabilities of brain injury phenotype using localized regression., Results: We included 2,440 patients, of whom 545 (23%) were awake, 1,065 (44%) had non-malignant coma, 548 (23%) had BSIB and 438 (18%) had cerebral edema. Only 92 (4%) had both BSIB and edema. Median CPR duration was 16 [IQR 8-28] minutes. Median CPR duration increased in a stepwise manner across groups: awake 6 [3-13] minutes; non-malignant coma 15 [8-25] minutes; BSIB 21 [13-31] minutes; cerebral edema 32 [22-46] minutes. Predicted probability of phenotype changes over time., Conclusions: Brain injury phenotype is related to CPR duration, which is a surrogate for severity of HIBI. The sequence of most likely primary HIBI phenotype with progressively longer CPR duration is awake, coma without BSIB or edema, BSIB, and finally cerebral edema., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)
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- 2023
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14. A Randomized Controlled Trial of OPT-302, a VEGF-C/D Inhibitor for Neovascular Age-Related Macular Degeneration.
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Jackson TL, Slakter J, Buyse M, Wang K, Dugel PU, Wykoff CC, Boyer DS, Gerometta M, Baldwin ME, and Price CF
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- Humans, Vascular Endothelial Growth Factor C therapeutic use, Antibodies, Monoclonal, Humanized adverse effects, Vascular Endothelial Growth Factor A, Angiogenesis Inhibitors, Intravitreal Injections, Treatment Outcome, Ranibizumab therapeutic use, Wet Macular Degeneration diagnosis, Wet Macular Degeneration drug therapy, Wet Macular Degeneration chemically induced
- Abstract
Purpose: Neovascular (wet) age-related macular degeneration (nAMD) is driven by VEGFs A, C, and D, which promote angiogenesis and vascular permeability. Intravitreal injections of anti-VEGF-A drugs are the standard of care, but these do not inhibit VEGF-C and D, which may explain why many patients fail to respond fully. This trial aimed to test the safety and efficacy of OPT-302, a biologic inhibitor of VEGF-C and D, in combination with the anti-VEGF-A inhibitor ranibizumab., Design: Dose-ranging, phase 2b, randomized, double-masked, sham-controlled trial., Participants: Participants with treatment-naive nAMD were enrolled from 109 sites across Europe, Israel, and the United States., Methods: Participants were randomized to 6, 4-weekly, intravitreal injections of 0.5 mg OPT-302, 2.0 mg OPT-302, or sham, plus intravitreal 0.5 mg ranibizumab., Main Outcome Measures: The primary outcome was mean change in ETDRS best-corrected visual acuity (BCVA) at 24 weeks. Secondary outcomes (comparing baseline with week 24) were the proportion of participants gaining or losing ≥ 15 ETDRS BCVA letters; area under the ETDRS BCVA over time curve; change in spectral-domain OCT (SD-OCT) central subfield thickness; and change in intraretinal fluid and subretinal fluid on SD-OCT., Results: Of 366 participants recruited from December 1, 2017, to November 30, 2018, 122, 123, and 121 were randomized to 0.5 mg OPT-302, 2.0 mg OPT-302, and sham, respectively. Mean (± standard deviation) visual acuity gain in the 2.0 mg OPT-302 group was significantly superior to sham (+14.2 ± 11.61 vs. +10.8 ± 11.52 letters; P = 0.01). The 0.5 mg OPT-302 group was not significantly different than the sham group (+9.44 ± 11.32 letters; P = 0.83). Compared with sham, the secondary BCVA outcomes favored the 2.0 mg OPT-302 group, with structural outcomes favoring both OPT-302 dosage groups. Adverse events (AEs) were similar across groups, with 16 (13.3%), 7 (5.6%), and 10 (8.3%) participants in the lower-dose, higher-dose, and sham groups, respectively, developing at least 1 serious AE. Two unrelated deaths both occurred in the sham arm., Conclusions: Significantly superior vision gain was observed with OPT-302 2.0 mg combination therapy, versus standard of care, with favorable safety (ClinicalTrials.gov identifier: NCT03345082)., Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references., (Copyright © 2023 American Academy of Ophthalmology. All rights reserved.)
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- 2023
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15. Deep learning of early brain imaging to predict post-arrest electroencephalography.
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Elmer J, Liu C, Pease M, Arefan D, Coppler PJ, Flickinger KL, Mettenburg JM, Baldwin ME, Barot N, and Wu S
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- Brain diagnostic imaging, Electroencephalography methods, Humans, Neuroimaging, Prognosis, Retrospective Studies, Deep Learning
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Introduction: Guidelines recommend use of computerized tomography (CT) and electroencephalography (EEG) in post-arrest prognostication. Strong associations between CT and EEG might obviate the need to acquire both modalities. We quantified these associations via deep learning., Methods: We performed a single-center, retrospective study including comatose patients hospitalized after cardiac arrest. We extracted brain CT DICOMs, resized and registered each to a standard anatomical atlas, performed skull stripping and windowed images to optimize contrast of the gray-white junction. We classified initial EEG as generalized suppression, other highly pathological findings or benign activity. We extracted clinical information available on presentation from our prospective registry. We trained three machine learning (ML) models to predict EEG from clinical covariates. We used three state-of-the-art approaches to build multi-headed deep learning models using similar model architectures. Finally, we combined the best performing clinical and imaging models. We evaluated discrimination in test sets., Results: We included 500 patients, of whom 218 (44%) had benign EEG findings, 135 (27%) showed generalized suppression and 147 (29%) had other highly pathological findings that were most commonly (93%) burst suppression with identical bursts. Clinical ML models had moderate discrimination (test set AUCs 0.73-0.80). Image-based deep learning performed worse (test set AUCs 0.51-0.69), particularly discriminating benign from highly pathological findings. Adding image-based deep learning to clinical models improved prediction of generalized suppression due to accurate detection of severe cerebral edema., Discussion: CT and EEG provide complementary information about post-arrest brain injury. Our results do not support selective acquisition of only one of these modalities, except in the most severely injured patients., (Copyright © 2022 Elsevier B.V. All rights reserved.)
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- 2022
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16. Awakening from post anoxic coma with burst suppression with identical bursts.
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Coppler PJ, Kusztos AE, Andreae M, Butcher BW, Doshi A, Baldwin ME, Barot N, Castellano JF, Fong-Isariyawongse JS, Urban A, Callaway CW, Steinberg A, and Elmer J
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Background: Electroencephalography (EEG) is commonly used after cardiac arrest. Burst suppression with identical bursts (BSIB) has been reported as a perfectly specific predictor of poor outcome but published case series are small. We describe two patients with BSIB who awakened from coma after cardiac arrest., Methods: We identified two out-of-hospital cardiac arrest (OHCA) patients with coma and BSIB. We determined the etiology of arrest, presenting neurological examination, potential confounders to neurological assessment, neurodiagnostics and time to awakening. We reviewed and interpreted EEGs using 2021 American Clinical Neurophysiology Society guidelines. We quantified identicality of bursts by calculating pairwise correlation coefficients between the first 500 ms of each aligned burst., Results: In case one we present a 62-year-old man with OHCA secondary to septic shock. EEG showed burst suppression pattern, with bursts consisted of high amplitude generalized spike waves in lock-step with myoclonus (inter-burst correlation = 0.86). He followed commands 3 days after arrest, when repeat EEG showed a continuous, variable and reactive background without epileptiform activity. Case two was a 49-year-old woman with OHCA secondary to polysubstance overdose. Initial EEG revealed burst suppression with high amplitude generalized polyspike-wave bursts with associated myoclonus. She followed commands on post-arrest day 4, when repeat EEG showed a continuous, variable and reactive background with frequent runs of bifrontal predominant sharply contoured rhythmic delta activity., Conclusion: These cases highlight the perils of prognosticating with a single modality in comatose cardiac arrest patients., (© 2021 The Author(s).)
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- 2021
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17. Sensitivity of Continuous Electroencephalography to Detect Ictal Activity After Cardiac Arrest.
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Elmer J, Coppler PJ, Solanki P, Westover MB, Struck AF, Baldwin ME, Kurz MC, and Callaway CW
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- Adult, Aged, Cohort Studies, Coma complications, Female, Humans, Male, Middle Aged, Out-of-Hospital Cardiac Arrest mortality, Seizures diagnosis, Time Factors, Electroencephalography methods, Monitoring, Physiologic methods, Out-of-Hospital Cardiac Arrest therapy, Seizures prevention & control
- Abstract
Importance: Epileptiform electroencephalographic (EEG) patterns are common after resuscitation from cardiac arrest, are associated with patient outcome, and may require treatment. It is unknown whether continuous EEG monitoring is needed to detect these patterns or if brief intermittent monitoring is sufficient. If continuous monitoring is required, the necessary duration of observation is unknown., Objective: To quantify the time-dependent sensitivity of continuous EEG for epileptiform event detection, and to compare continuous EEG to several alternative EEG-monitoring strategies for post-cardiac arrest outcome prediction., Design, Setting, and Participants: This observational cohort study was conducted in 2 academic medical centers between September 2010 and January 2018. Participants included 759 adults who were comatose after being resuscitated from cardiac arrest and who underwent 24 hours or more of EEG monitoring., Main Outcomes and Measures: Epileptiform EEG patterns associated with neurological outcome at hospital discharge, such as seizures likely to cause secondary injury., Results: Overall, 759 patients were included in the analysis; 281 (37.0%) were female, and the mean (SD) age was 58 (17) years. Epileptiform EEG activity was observed in 414 participants (54.5%), of whom only 26 (3.4%) developed potentially treatable seizures. Brief intermittent EEG had an estimated 66% (95% CI, 62%-69%) to 68% (95% CI, 66%-70%) sensitivity for detection of prognostic epileptiform events. Depending on initial continuity of the EEG background, 0 to 51 hours of monitoring were needed to achieve 95% sensitivity for the detection of prognostic epileptiform events. Brief intermittent EEG had a sensitivity of 7% (95% CI, 4%-12%) to 8% (95% CI, 4%-12%) for the detection of potentially treatable seizures, and 0 to 53 hours of continuous monitoring were needed to achieve 95% sensitivity for the detection of potentially treatable seizures. Brief intermittent EEG results yielded similar information compared with continuous EEG results when added to multivariable models predicting neurological outcome., Conclusions and Relevance: Compared with continuous EEG monitoring, brief intermittent monitoring was insensitive for detection of epileptiform events. Monitoring EEG results significantly improved multimodality prediction of neurological outcome, but continuous monitoring appeared to add little additional information compared with brief intermittent monitoring.
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- 2020
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18. Phase 1 Study of OPT-302 Inhibition of Vascular Endothelial Growth Factors C and D for Neovascular Age-Related Macular Degeneration.
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Dugel PU, Boyer DS, Antoszyk AN, Steinle NC, Varenhorst MP, Pearlman JA, Gillies MC, Finger RP, Baldwin ME, and Leitch IM
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- Aged, Female, Fluorescein Angiography methods, Follow-Up Studies, Fundus Oculi, Humans, Macula Lutea pathology, Male, Prospective Studies, Tomography, Optical Coherence methods, Visual Acuity, Wet Macular Degeneration diagnosis, Wet Macular Degeneration metabolism, Angiogenesis Inhibitors administration & dosage, Vascular Endothelial Growth Factor C antagonists & inhibitors, Vascular Endothelial Growth Factor D antagonists & inhibitors, Wet Macular Degeneration drug therapy
- Abstract
Purpose: OPT-302 is a novel inhibitor of vascular endothelial growth factor (VEGF)-C and VEGF-D. A phase 1 trial assessed the safety of intravitreal OPT-302 as monotherapy or combined with ranibizumab (Lucentis; Genentech, South San Francisco, CA) in patients with neovascular age-related macular degeneration (nAMD)., Design: Open-label, dose escalation followed by a randomized dose expansion., Participants: Fifty-one patients with nAMD who were either treatment naïve (n = 25) or previously were treated with anti-VEGF A therapy (n = 26)., Methods: In the dose escalation, groups of 5 patients in 4 cohorts received ascending doses of OPT-302 (0.3 mg, 1 mg, or 2 mg) in combination with ranibizumab (0.5 mg), or as monotherapy (2 mg). In the dose expansion, 31 patients were randomized (3:1) to OPT-302 (2 mg) in combination with ranibizumab (n = 23) or as monotherapy (n = 8). Participants received three intravitreal treatments of OPT-302 once every 4 weeks either with or without ranibizumab., Main Outcome Measures: Safety and tolerability, OPT-302 pharmacokinetics and immunogenicity, effects on best-corrected visual acuity (BCVA), and anatomic changes., Results: Intravitreal OPT-302 with or without ranibizumab was well tolerated with low systemic exposure, no dose-limiting toxicities and no immunogenicity. In patients receiving OPT-302 monotherapy, 7 of 13 (54%) did not require rescue anti-VEGF-A therapy and the mean change in BCVA from baseline to week 12 was +5.6 letters (range, 0-18 letters). Mean BCVA gains from baseline to week 12 following combination OPT-302 with ranibizumab were +10.8 letters (95% confidence interval [CI], 4-17; n = 18) in treatment-naïve patients and +4.9 letters (95% CI, 3-7; n = 19) in previously treated patients, respectively. Corresponding reductions in mean central subfield thickness at week 12 in both groups were -119 μm (95% CI, -176 to -62 μm) and -54 μm (95% CI, -82 to -26 μm), respectively, whilst 50% of treatment-naïve patients also showed no detectable choroidal neovascularization at week 12 on fluorescein angiography., Conclusions: Intravitreal OPT-302 inhibition of VEGF-C and -D was well tolerated, and OPT-302 combination therapy may overcome an escape mechanism to VEGF-A suppression in the management of nAMD., (Copyright © 2019 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.)
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- 2020
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19. Features of Simultaneous Scalp and Intracranial EEG That Predict Localization of Ictal Onset Zone.
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Abramovici S, Antony A, Baldwin ME, Urban A, Ghearing G, Pan J, Sun T, Krafty RT, Richardson RM, and Bagic A
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- Adolescent, Adult, Epilepsies, Partial physiopathology, Epilepsy physiopathology, Epilepsy surgery, Female, Humans, Magnetic Resonance Imaging methods, Male, Middle Aged, Seizures physiopathology, Treatment Outcome, Young Adult, Electroencephalography methods, Epilepsies, Partial surgery, Scalp physiopathology, Seizures surgery
- Abstract
Objective: To assess the utility of simultaneous scalp EEG in patients with focal epilepsy undergoing intracranial EEG evaluation after a detailed presurgical testing, including an inpatient scalp video EEG evaluation., Methods: Patients who underwent simultaneous scalp and intracranial EEG (SSIEEG) monitoring were classified into group 1 or 2 depending on whether the seizure onset zone was delineated or not. Seizures were analyzed using the following 3 EEG features at the onset of seizures latency, location, and pattern., Results: The criteria showed at least one of the following features when comparing SSIEEG: prolonged latency, absence of anatomical congruence, lack of concordance of EEG pattern in 11.11% (1/9) of the patients in group 1 and 75 % (3/4) of the patients in group 2. These 3 features were not present in any of the 5 patients who had Engel class I outcome compared with 1 of the 2 patients (50%) who had seizure recurrence after resective surgery. The mean latency of seizure onset in scalp EEG compared with intracranial EEG of patients in group 1 was 17.48 seconds (SD = 16.07) compared with 4.33 seconds (SD = 11.24) in group 2 ( P = .03). None of the seizures recorded in patients in group 1 had a discordant EEG pattern in SSIEEG., Conclusion: Concordance in EEG features like latency, location, and EEG pattern, at the onset of seizures in SSIEEG is associated with a favorable outcome after epilepsy surgery in patients with intractable focal epilepsy., Significance: Simultaneous scalp EEG complements intracranial EEG evaluation even after a detailed inpatient scalp video EEG evaluation and could be part of standard intracranial EEG studies in patients with intractable focal epilepsy.
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- 2018
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20. Response to "A critique for the new Canadian FASD diagnostic Guidelines".
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Cook JL, Green CR, Lilley C, Psych R, Anderson S, Baldwin ME, Chudley AE, Conry J, LeBlanc N, Loock CA, Mallon B, McFarlane A, Temple V, and Psych C
- Published
- 2018
21. Effect of sedation on quantitative electroencephalography after cardiac arrest.
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Drohan CM, Cardi AI, Rittenberger JC, Popescu A, Callaway CW, Baldwin ME, and Elmer J
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- Adult, Aged, Coma etiology, Coma mortality, Coma therapy, Female, Humans, Male, Middle Aged, Out-of-Hospital Cardiac Arrest complications, Out-of-Hospital Cardiac Arrest mortality, Prospective Studies, Retrospective Studies, Electroencephalography drug effects, Hypnotics and Sedatives administration & dosage, Out-of-Hospital Cardiac Arrest therapy
- Abstract
Background: Electroencephalography (EEG) has clinical and prognostic importance after cardiac arrest (CA). Recently, interest in quantitative EEG (qEEG) analysis has grown. The qualitative effects of sedation on EEG are well known, but potentially confounding effects of sedatives on qEEG after anoxic injury are poorly characterized. We hypothesize that sedation increases suppression ratio (SR) and decreases alpha/delta ratio (ADR) and amplitude-integrated EEG (aEEG), and that the magnitude of sedation effects will be associated with outcome., Methods: We routinely monitor comatose post-arrest patients with EEG for 48-72h. We included comatose EEG-monitored patients after CA who had protocolized daily sedation interruptions. We used Persyst v12 to quantify qEEG parameters and calculated medians for 10min immediately prior to sedation interruption and for the last 5min of interruption. We used paired t-tests to determine whether qEEG parameters changed with sedation cessation, and logistic regression to determine whether these changes predicted functional recovery or survival at discharge., Results: 78 subjects were included (median age 56, 65% male). Interruptions occurred a median duration of 34h post-arrest and lasted a median duration of 60min. Prior to interruption, higher aEEG predicted survival, while lower SR predicted both survival and favorable outcome. During interruption, SR decreased (p<0.001), aEEG increased (p=0.002), and ADR did not change. Larger decreases in SR predicted decreased survival (OR=1.04 per percent change; 95% CI 1.00-1.09)., Conclusion: Higher aEEG and lower SR predict survival after CA. Sedation alters aEEG and SR, but importantly does not appear to affect the relationship between these parameter values and outcome., (Copyright © 2017 Elsevier B.V. All rights reserved.)
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- 2018
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22. Misleading EEG Lateralization Associated With Midline Shift.
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Ghearing GR, Abramovici S, Popescu A, and Baldwin ME
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- Aged, Brain diagnostic imaging, Epilepsy diagnostic imaging, Epilepsy etiology, Female, Humans, Male, Middle Aged, Retrospective Studies, Tomography, X-Ray Computed, Brain physiopathology, Electroencephalography, Epilepsy physiopathology, Functional Laterality
- Abstract
Midline discharges, lateralized periodic discharges, and seizures have been described with ipsilateral lesions that result in midline shift (MLS). Periodic discharges and seizures arising contralateral to a known lesion have not previously been described as a sign of MLS. We present four patients with focal brain lesions, resulting in MLS and epileptiform discharges arising from the contralateral hemisphere. Patient 1 underwent a right anterior temporal lobectomy. On postoperative day 2, computed tomography demonstrated a right to left MLS of 12 mm, and EEG was remarkable for left temporal nonconvulsive status epilepticus. Patient 2 experienced a subarachnoid hemorrhage, which was more prominent on the left. Computed tomography after craniotomy demonstrated left to right MLS of 6 mm, and EEG was remarkable for right lateralized periodic discharges. Patient 3 had a right subdural hematoma and underwent craniotomy for evacuation. On postoperative day 3, computed tomography demonstrated a right MLS of 7 mm, and EEG was remarkable for left temporal nonconvulsive status epilepticus. Patient 4 had traumatic brain hemorrhages with maximal left frontotemporal involvement. Six days after the trauma, computed tomography was significant for left to right MLS of 9 mm, and EEG showed right lateralized periodic discharges. Epileptiform discharges and seizures occurring contralateral to a known lesion may be an indicator of MLS.
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- 2017
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23. Group-Based Trajectory Modeling of Suppression Ratio After Cardiac Arrest.
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Elmer J, Gianakas JJ, Rittenberger JC, Baldwin ME, Faro J, Plummer C, Shutter LA, Wassel CL, Callaway CW, and Fabio A
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- Adult, Aged, Female, Humans, Male, Middle Aged, Models, Neurological, Prognosis, Coma physiopathology, Electroencephalography methods, Heart Arrest physiopathology, Hypoxia, Brain physiopathology
- Abstract
Background: Existing studies of quantitative electroencephalography (qEEG) as a prognostic tool after cardiac arrest (CA) use methods that ignore the longitudinal pattern of qEEG data, resulting in significant information loss and precluding analysis of clinically important temporal trends. We tested the utility of group-based trajectory modeling (GBTM) for qEEG classification, focusing on the specific example of suppression ratio (SR)., Methods: We included comatose CA patients hospitalized from April 2010 to October 2014, excluding CA from trauma or neurological catastrophe. We used Persyst
® v12 to generate SR trends and used semi-quantitative methods to choose appropriate sampling and averaging strategies. We used GBTM to partition SR data into different trajectories and regression associate trajectories with outcome. We derived a multivariate logistic model using clinical variables without qEEG to predict survival, then added trajectories and/or non-longitudinal SR estimates, and assessed changes in model performance., Results: Overall, 289 CA patients had ≥36 h of EEG yielding 10,404 h of data (mean age 57 years, 81 % arrested out-of-hospital, 33 % shockable rhythms, 31 % overall survival, 17 % discharged to home or acute rehabilitation). We identified 4 distinct SR trajectories associated with survival (62, 26, 12, and 0 %, P < 0.0001 across groups) and CPC (35, 10, 4, and 0 %, P < 0.0001 across groups). Adding trajectories significantly improved model performance compared to adding non-longitudinal data., Conclusions: Longitudinal analysis of continuous qEEG data using GBTM provides more predictive information than analysis of qEEG at single time-points after CA., Competing Interests: The authors have no additional funding or conflicts of interest to report.- Published
- 2016
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24. Continuous EEG monitoring enhances multimodal outcome prediction in hypoxic-ischemic brain injury.
- Author
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Amorim E, Rittenberger JC, Zheng JJ, Westover MB, Baldwin ME, Callaway CW, and Popescu A
- Subjects
- Adult, Aged, Female, Heart Arrest mortality, Hospital Mortality, Humans, Hypothermia, Induced, Hypoxia-Ischemia, Brain complications, Male, Middle Aged, Predictive Value of Tests, Prospective Studies, ROC Curve, Status Epilepticus complications, Coma mortality, Electroencephalography, Hypoxia-Ischemia, Brain mortality, Neurophysiological Monitoring methods
- Abstract
Objective: Hypoxic brain injury is the largest contributor to disability and mortality after cardiac arrest. We aim to identify electroencephalogram (EEG) characteristics that can predict outcome on cardiac arrest patients treated with targeted temperature management (TTM)., Methods: We retrospectively examined clinical, EEG, functional outcome at discharge, and in-hospital mortality for 373 adult subjects with return of spontaneous circulation after cardiac arrest. Poor outcome was defined as a Cerebral Performance Category score of 3-5. Pure suppression-burst (SB) was defined as SB not associated with status epilepticus (SE), seizures, or generalized periodic discharges., Results: In-hospital mortality was 68.6% (N=256). Presence of both unreactive EEG background and SE was associated with a positive predictive value (PPV) of 100% (95% confidence interval: 0.96-1) and a false-positive rate (FPR) of 0% (95% CI: 0-0.11) for poor functional outcome. A prediction model including demographics data, admission exam, presence of status epilepticus, pure SB, and lack of EEG reactivity had an area under the curve of 0.92 (95% CI: 0.87-0.95) for poor functional outcome prediction, and 0.96 (95% CI: 0.94-0.98) for in-hospital mortality. Presence of pure SB (N=87) was confounded by anesthetics use in 83.9% of the cases, and was not an independent predictor of poor functional outcome, having a FPR of 23% (95% CI: 0.19-0.28)., Conclusions: An unreactive EEG background and SE predicted poor functional outcome and in-hospital mortality in cardiac arrest patients undergoing TTM. Prognostic value of pure SB is confounded by use of sedative agents, and its use on prognostication decisions should be made with caution., Competing Interests: E.A, J.C.R., J.J.Z., M.B.W., M.E.B., C.W.C, A.P. report no disclosures relevant to the manuscript, (Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.)
- Published
- 2016
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25. Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan.
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Cook JL, Green CR, Lilley CM, Anderson SM, Baldwin ME, Chudley AE, Conry JL, LeBlanc N, Loock CA, Lutke J, Mallon BF, McFarlane AA, Temple VK, and Rosales T
- Subjects
- Advisory Committees, Alcohol Drinking, Canada, Child, Child, Preschool, Female, Focus Groups, Humans, Infant, Infant, Newborn, Male, Mass Screening, Pregnancy, Referral and Consultation, Algorithms, Fetal Alcohol Spectrum Disorders diagnosis, Patient Care Team, Practice Guidelines as Topic
- Published
- 2016
- Full Text
- View/download PDF
26. Malignant EEG patterns in cardiac arrest patients treated with targeted temperature management who survive to hospital discharge.
- Author
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Amorim E, Rittenberger JC, Baldwin ME, Callaway CW, and Popescu A
- Subjects
- Age Factors, Anesthetics, Intravenous therapeutic use, Body Temperature physiology, Heart Arrest physiopathology, Humans, Middle Aged, Patient Discharge, Patient Outcome Assessment, Prospective Studies, Rewarming, Electroencephalography, Heart Arrest therapy, Hypothermia, Induced, Neurophysiological Monitoring, Seizures physiopathology, Status Epilepticus physiopathology
- Abstract
Background and Purpose: Cardiac arrest patients treated with targeted temperature management (TTM) have improved neurological outcomes, however mortality remains high. EEG monitoring improves detection of malignant EEG patterns (MEPs), however their prevalence in patients surviving to hospital discharge is unknown., Design/methods: We examined consecutive cardiac arrest subjects who received TTM and continuous EEG monitoring at one academic center. Only subjects surviving to hospital discharge were included in the analysis. MEPs were defined as seizures, status epilepticus, myoclonic status epilepticus, or generalized periodic discharges. Subjects with suppression-burst (SB) without concomitant MEPs were categorized as having a "pure" SB pattern. Demographic, survival, hospital discharge disposition, and neurological function data were recorded retrospectively. Outcomes were assessed using the Glasgow-Pittsburgh Cerebral Performance Category (CPC). A CPC score of 1-2 was considered "good" neurological function, and a CPC of 3-4 "poor"., Results: Of 364 admissions due to cardiac arrest screened, 120 (29.9%) survived to hospital discharge and met inclusion criteria. MEPs and pure SB were observed in 19 (15.8%) and 22 (18.3%) survivors respectively. Two subjects with MEP and eight subjects with pure SB had good neurological function at discharge, however all SB cases were confounded by the use of anesthetic agents. Presence of MEPs was not an independent predictor of poor neurological function (p=0.1)., Conclusions: MEPs are common among cardiac arrest patients treated with induced hypothermia who survive to hospital discharge. Poor neurological function at discharge was not associated with MEPs. Prospective studies assessing the role of EEG monitoring in cardiac arrest prognostication are warranted., (Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.)
- Published
- 2015
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27. The care of the baby's eyes in the perambulator.
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Baldwin ME
- Subjects
- History, 19th Century, Humans, Infant, Eye Protective Devices history, Infant Care history, Infant Equipment history
- Published
- 2015
- Full Text
- View/download PDF
28. Differential expression of VEGF ligands and receptors in prostate cancer.
- Author
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Woollard DJ, Opeskin K, Coso S, Wu D, Baldwin ME, and Williams ED
- Subjects
- Blood Vessels metabolism, Blood Vessels pathology, Humans, Immunohistochemistry, Lymphangiogenesis physiology, Lymphatic Metastasis pathology, Lymphatic Vessels metabolism, Lymphatic Vessels pathology, Male, Neoplasm Grading, Neovascularization, Pathologic metabolism, Neovascularization, Pathologic pathology, Prostate blood supply, Prostate metabolism, Prostate pathology, Prostatic Neoplasms secondary, Signal Transduction physiology, Vascular Endothelial Growth Factor C metabolism, Vascular Endothelial Growth Factor D metabolism, Prostatic Neoplasms metabolism, Vascular Endothelial Growth Factor A metabolism, Vascular Endothelial Growth Factor Receptor-1 metabolism, Vascular Endothelial Growth Factor Receptor-2 metabolism, Vascular Endothelial Growth Factor Receptor-3 metabolism
- Abstract
Background: Prostate cancer disseminates to regional lymph nodes, however the molecular mechanisms responsible for lymph node metastasis are poorly understood. The vascular endothelial growth factor (VEGF) ligand and receptor family have been implicated in the growth and spread of prostate cancer via activation of the blood vasculature and lymphatic systems. The purpose of this study was to comprehensively examine the expression pattern of VEGF ligands and receptors in the glandular epithelium, stroma, lymphatic vasculature and blood vessels in prostate cancer., Methods: The localization of VEGF-A, VEGF-C, VEGF-D, VEGF receptor (VEGFR)-1, VEGFR-2, and VEGFR-3 was examined in cancerous and adjacent benign prostate tissue from 52 subjects representing various grades of prostate cancer., Results: Except for VEGFR-2, extensive staining was observed for all ligands and receptors in the prostate specimens. In epithelial cells, VEGF-A and VEGFR-1 expression was higher in tumor tissue compared to benign tissue. VEGF-D and VEGFR-3 expression was significantly higher in benign tissue compared to tumor in the stroma and the endothelium of lymphatic and blood vessels. In addition, the frequency of lymphatic vessels, but not blood vessels, was lower in tumor tissue compared with benign tissue., Conclusions: These results suggest that activation of VEGFR-1 by VEGF-A within the carcinoma, and activation of lymphatic endothelial cell VEGFR-3 by VEGF-D within the adjacent benign stroma may be important signaling mechanisms involved in the progression and subsequent metastatic spread of prostate cancer. Thus inhibition of these pathways may contribute to therapeutic strategies for the management of prostate cancer., (Copyright © 2012 Wiley Periodicals, Inc.)
- Published
- 2013
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29. VEGF-D promotes tumor metastasis by regulating prostaglandins produced by the collecting lymphatic endothelium.
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Karnezis T, Shayan R, Caesar C, Roufail S, Harris NC, Ardipradja K, Zhang YF, Williams SP, Farnsworth RH, Chai MG, Rupasinghe TW, Tull DL, Baldwin ME, Sloan EK, Fox SB, Achen MG, and Stacker SA
- Subjects
- Animals, Anti-Inflammatory Agents pharmacology, Endothelium, Lymphatic pathology, Female, Gene Expression Regulation, Neoplastic drug effects, Humans, Lymphangiogenesis drug effects, Lymphatic Metastasis genetics, Lymphatic System drug effects, Lymphatic System pathology, Lymphatic Vessels metabolism, Lymphatic Vessels pathology, Mice, Mice, Inbred NOD, Mice, SCID, Vascular Endothelial Growth Factor D genetics, Vascular Endothelial Growth Factor D metabolism, Vascular Endothelial Growth Factor Receptor-2 metabolism, Vascular Endothelial Growth Factor Receptor-3 metabolism, Cell Transformation, Neoplastic, Endothelium, Lymphatic metabolism, Lymphatic Metastasis physiopathology, Prostaglandins metabolism, Vascular Endothelial Growth Factor D physiology
- Abstract
Lymphatic metastasis is facilitated by lymphangiogenic growth factors VEGF-C and VEGF-D that are secreted by some primary tumors. We identified regulation of PGDH, the key enzyme in prostaglandin catabolism, in endothelial cells of collecting lymphatics, as a key molecular change during VEGF-D-driven tumor spread. The VEGF-D-dependent regulation of the prostaglandin pathway was supported by the finding that collecting lymphatic vessel dilation and subsequent metastasis were affected by nonsteroidal anti-inflammatory drugs (NSAIDs), known inhibitors of prostaglandin synthesis. Our data suggest a control point for cancer metastasis within the collecting lymphatic endothelium, which links VEGF-D/VEGFR-2/VEGFR-3 and the prostaglandin pathways. Collecting lymphatics therefore play an active and important role in metastasis and may provide a therapeutic target to restrict tumor spread., (Copyright © 2012 Elsevier Inc. All rights reserved.)
- Published
- 2012
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30. Visual-evoked potentials for intraoperative neurophysiology monitoring: another flash in the pan?
- Author
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Cohen BA and Baldwin ME
- Published
- 2011
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31. Deletion of vascular endothelial growth factor C (VEGF-C) and VEGF-D is not equivalent to VEGF receptor 3 deletion in mouse embryos.
- Author
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Haiko P, Makinen T, Keskitalo S, Taipale J, Karkkainen MJ, Baldwin ME, Stacker SA, Achen MG, and Alitalo K
- Subjects
- Alleles, Animals, Blood Vessels embryology, Embryo, Mammalian abnormalities, Embryo, Mammalian pathology, Gene Targeting, Lymphangiogenesis, Lymphatic Vessels abnormalities, Lymphatic Vessels embryology, Lymphatic Vessels pathology, Mice, Mice, Knockout, Phenotype, Embryo, Mammalian metabolism, Gene Deletion, Vascular Endothelial Growth Factor C deficiency, Vascular Endothelial Growth Factor D deficiency, Vascular Endothelial Growth Factor Receptor-3 deficiency
- Abstract
Lymphatic vessels play an important role in the regulation of tissue fluid balance, immune responses, and fat adsorption and are involved in diseases including lymphedema and tumor metastasis. Vascular endothelial growth factor (VEGF) receptor 3 (VEGFR-3) is necessary for development of the blood vasculature during early embryogenesis, but later, VEGFR-3 expression becomes restricted to the lymphatic vasculature. We analyzed mice deficient in both of the known VEGFR-3 ligands, VEGF-C and VEGF-D. Unlike the Vegfr3(-/-) embryos, the Vegfc(-/-); Vegfd(-/-) embryos displayed normal blood vasculature after embryonic day 9.5. Deletion of Vegfr3 in the epiblast, using keratin 19 (K19) Cre, resulted in a phenotype identical to that of the Vegfr3(-/-) embryos, suggesting that this phenotype is due to defects in the embryo proper and not in placental development. Interestingly, the Vegfr3(neo) hypomorphic mutant mice carrying the neomycin cassette between exons 1 and 2 showed defective lymphatic development. Overexpression of human or mouse VEGF-D in the skin, under the K14 promoter, rescued the lymphatic hypoplasia of the Vegfc(+/-) mice in the K14-VEGF-D; Vegfc(+/-) compound mice, suggesting that VEGF-D is functionally redundant with VEGF-C in the stimulation of developmental lymphangiogenesis. Our results suggest VEGF-C- and VEGF-D-independent functions for VEGFR-3 in the early embryo.
- Published
- 2008
- Full Text
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32. Manganese cumulative exposure and symptoms: a follow-up study of alloy workers.
- Author
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Bouchard M, Mergler D, Baldwin ME, and Panisset M
- Subjects
- Adult, Aged, Autonomic Nervous System Diseases chemically induced, Fatigue chemically induced, Follow-Up Studies, Humans, Male, Memory Disorders chemically induced, Middle Aged, Movement Disorders etiology, Retrospective Studies, Surveys and Questionnaires, Alloys, Manganese Poisoning epidemiology, Manganese Poisoning physiopathology, Occupational Exposure statistics & numerical data
- Abstract
Long-term exposure to manganese (Mn) particulates through inhalation can be neurotoxic, with deficits in neuromotor and cognitive domains. Mn-exposed individuals also report symptoms, including fatigue, mood changes, irritability, concentration difficulties, and sweating in the absence of physical effort. The long-term course of Mn-related symptoms after cessation of exposure has never been examined. Male workers from a Mn-alloy production plant participated in a study on nervous system functions (initial examination), and were followed-up 14 years after plant closure. The relation between self-reported symptoms and Mn cumulative exposure index (CEI) was examined among 71 Mn-alloy workers and 71 referents. Symptoms from the questionnaire were grouped into categories, and the reported frequency was compared between referents and Mn-alloy workers in each Mn CEI tertile using General Linear Models, controlling for age, education, and alcohol consumption. A gradual increase in symptoms frequency was observed for complaints related to hearing and movement control both at initial and follow-up examination, and fatigue and autonomic nervous system only at initial examination. In addition, an exposure-effect relation was apparent for symptoms related to memory, concentration and balance reported at both examinations, with Mn-workers in the highest CEI tertile reporting the highest level of symptomatology. Sleeping complaints were not associated with exposure to Mn, while musculoskeletal pain and muscular weakness were reported more often by Mn-workers than referents but were not clearly related to CEI. The findings suggest that former Mn-alloy workers continue to perceive symptoms many years after cessation of exposure. Despite the limitations of self-reported symptoms, subjective complaints are an important part of a health assessment since they relate directly to perceived health status and day-to-day functioning.
- Published
- 2008
- Full Text
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33. Tumor refractoriness to anti-VEGF treatment is mediated by CD11b+Gr1+ myeloid cells.
- Author
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Shojaei F, Wu X, Malik AK, Zhong C, Baldwin ME, Schanz S, Fuh G, Gerber HP, and Ferrara N
- Subjects
- Animals, Cell Line, Tumor, Drug Resistance, Neoplasm, Mice, Mice, Inbred C57BL, Treatment Outcome, Antineoplastic Agents administration & dosage, CD11b Antigen metabolism, Leukemia, Myeloid drug therapy, Leukemia, Myeloid metabolism, Neovascularization, Pathologic drug therapy, Neovascularization, Pathologic metabolism, Receptors, Chemokine metabolism, Vascular Endothelial Growth Factor A antagonists & inhibitors
- Abstract
Vascular endothelial growth factor (VEGF) is an essential regulator of normal and abnormal blood vessel growth. A monoclonal antibody (mAb) that targets VEGF suppresses tumor growth in murine cancer models and human patients. We investigated cellular and molecular events that mediate refractoriness of tumors to anti-angiogenic therapy. Inherent anti-VEGF refractoriness is associated with infiltration of the tumor tissue by CD11b+Gr1+ myeloid cells. Recruitment of these myeloid cells is also sufficient to confer refractoriness. Combining anti-VEGF treatment with a mAb that targets myeloid cells inhibits growth of refractory tumors more effectively than anti-VEGF alone. Gene expression analysis in CD11b+Gr1+ cells isolated from the bone marrow of mice bearing refractory tumors reveals higher expression of a distinct set of genes known to be implicated in active mobilization and recruitment of myeloid cells. These findings indicate that, in our models, refractoriness to anti-VEGF treatment is determined by the ability of tumors to prime and recruit CD11b+Gr1+ cells.
- Published
- 2007
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34. Phosphorylation of the NF2 tumor suppressor in Schwann cells is mediated by Cdc42-Pak and requires paxillin binding.
- Author
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Thaxton C, Lopera J, Bott M, Baldwin ME, Kalidas P, and Fernandez-Valle C
- Subjects
- Animals, Animals, Newborn, Cells, Cultured, Enzyme Activation, Gene Expression Regulation, Green Fluorescent Proteins metabolism, Immunohistochemistry, Immunoprecipitation, Mutagenesis, Phosphorylation, Protein Binding, Rats, Transfection, Neurofibromatosis 2 metabolism, Neurofibromin 2 metabolism, Paxillin metabolism, Protein Serine-Threonine Kinases metabolism, Schwann Cells metabolism, cdc42 GTP-Binding Protein metabolism
- Abstract
Mutations in the Neurofibromatosis type 2 tumor suppressor gene that encodes Schwannomin causes formation of benign schwannomas. Schwannoma cells lose their characteristic bipolar shape and become rounded with excessive ruffling membranes. Schwannomin is phosphorylated at serine 518 (S518) by p21 activated kinase (Pak). Unphosphorylated schwannomin is associated with growth inhibition but little is known about the function of the phosphorylated form, or the molecular events leading to its phosphorylation. Here, we report in SCs that schwannomin S518 phosphorylation requires binding to paxillin and targeting to the plasma membrane. Phospho-S518-schwannomin is enriched in the peripheral-most aspects of membrane specializations where paxillin, activated Pak, Cdc42 but not Rac are highly expressed. Schwannomin and Pak phosphorylation levels are not reduced in response to lowering Rac-GTP levels with NSC23766. Expression of schwannomin S518A/D-GFP variants each distinctively altered Schwann cell shape and polarity. These results are consistent with tight spatial regulation of S518 phosphorylation at the plasma membrane in a paxillin and Cdc42-Pak dependent manner that leads to local reorganization of the SC cytoskeleton.
- Published
- 2007
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35. Molecular pathways for lymphangiogenesis and their role in human disease.
- Author
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Stacker SA, Farnsworth RH, Karnezis T, Shayan R, Smith DP, Paavonen K, Davydova N, Caesar C, Inder R, Baldwin ME, McColl BK, Roufail S, Williams RA, Hughes RA, Alitalo K, and Achen MG
- Subjects
- Humans, Lymphangiogenesis genetics, Signal Transduction genetics, Lymphangiogenesis physiology, Neoplasms metabolism, Signal Transduction physiology, Vascular Endothelial Growth Factors metabolism
- Abstract
The lymphatic network functions to return fluid, cells and macromolecules to the circulation. Recent characterization of growth factors that control the growth and development of the lymphatics, and markers which specify lymphatic endothelial cells have enhanced our understanding of this system. Members of the VEGF family of factors are key regulators of these vessels with VEGF-C/VEGF-D and VEGFR-3 being the best validated signalling pathways in lymphangiogenesis. The study of these molecules in various pathologies has shown that they are important in the processes of cancer metastasis and in the formation of lymphoedema. Knowledge of these molecular pathways allows for the generation of modulators of these pathways which could form the basis of novel therapeutic approaches.
- Published
- 2007
- Full Text
- View/download PDF
36. Corneal avascularity is due to soluble VEGF receptor-1.
- Author
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Ambati BK, Nozaki M, Singh N, Takeda A, Jani PD, Suthar T, Albuquerque RJ, Richter E, Sakurai E, Newcomb MT, Kleinman ME, Caldwell RB, Lin Q, Ogura Y, Orecchia A, Samuelson DA, Agnew DW, St Leger J, Green WR, Mahasreshti PJ, Curiel DT, Kwan D, Marsh H, Ikeda S, Leiper LJ, Collinson JM, Bogdanovich S, Khurana TS, Shibuya M, Baldwin ME, Ferrara N, Gerber HP, De Falco S, Witta J, Baffi JZ, Raisler BJ, and Ambati J
- Subjects
- Animals, Gene Deletion, Mice, Neovascularization, Physiologic, RNA, Messenger genetics, RNA, Messenger metabolism, Solubility, Trichechus, Vascular Endothelial Growth Factor A metabolism, Vascular Endothelial Growth Factor Receptor-1 deficiency, Vascular Endothelial Growth Factor Receptor-1 genetics, Cornea blood supply, Cornea metabolism, Vascular Endothelial Growth Factor Receptor-1 metabolism
- Abstract
Corneal avascularity-the absence of blood vessels in the cornea-is required for optical clarity and optimal vision, and has led to the cornea being widely used for validating pro- and anti-angiogenic therapeutic strategies for many disorders. But the molecular underpinnings of the avascular phenotype have until now remained obscure and are all the more remarkable given the presence in the cornea of vascular endothelial growth factor (VEGF)-A, a potent stimulator of angiogenesis, and the proximity of the cornea to vascularized tissues. Here we show that the cornea expresses soluble VEGF receptor-1 (sVEGFR-1; also known as sflt-1) and that suppression of this endogenous VEGF-A trap by neutralizing antibodies, RNA interference or Cre-lox-mediated gene disruption abolishes corneal avascularity in mice. The spontaneously vascularized corneas of corn1 and Pax6+/- mice and Pax6+/- patients with aniridia are deficient in sflt-1, and recombinant sflt-1 administration restores corneal avascularity in corn1 and Pax6+/- mice. Manatees, the only known creatures uniformly to have vascularized corneas, do not express sflt-1, whereas the avascular corneas of dugongs, also members of the order Sirenia, elephants, the closest extant terrestrial phylogenetic relatives of manatees, and other marine mammals (dolphins and whales) contain sflt-1, indicating that it has a crucial, evolutionarily conserved role. The recognition that sflt-1 is essential for preserving the avascular ambit of the cornea can rationally guide its use as a platform for angiogenic modulators, supports its use in treating neovascular diseases, and might provide insight into the immunological privilege of the cornea.
- Published
- 2006
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37. Redundant roles of VEGF-B and PlGF during selective VEGF-A blockade in mice.
- Author
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Malik AK, Baldwin ME, Peale F, Fuh G, Liang WC, Lowman H, Meng G, Ferrara N, and Gerber HP
- Subjects
- Animals, Animals, Newborn, Antibodies, Monoclonal pharmacology, Gene Expression Regulation, Developmental, Humans, Mice, Mice, Mutant Strains, Mice, Nude, Neoplasms, Experimental blood supply, Neoplasms, Experimental metabolism, Placenta Growth Factor, Pregnancy Proteins antagonists & inhibitors, Pregnancy Proteins immunology, Survival Rate, Vascular Endothelial Growth Factor A immunology, Vascular Endothelial Growth Factor A metabolism, Vascular Endothelial Growth Factor B antagonists & inhibitors, Vascular Endothelial Growth Factor B immunology, Vascular Endothelial Growth Factor Receptor-1 genetics, Vascular Endothelial Growth Factor Receptor-1 immunology, Vascular Endothelial Growth Factor Receptor-1 metabolism, Neoplasms, Experimental therapy, Neovascularization, Pathologic, Pregnancy Proteins metabolism, Vascular Endothelial Growth Factor A antagonists & inhibitors, Vascular Endothelial Growth Factor B metabolism
- Abstract
Vascular endothelial growth factor-A (VEGF-A) and its 2 transmembrane tyrosine-kinase receptors, VEGFR-1 and VEGFR-2, constitute a ligand-receptor signaling system that is crucial for developmental angiogenesis. VEGF-B and placental growth factor (PlGF) activate VEGFR-1 selectively, however, mice lacking either ligand display only minor developmental defects. We hypothesized that the relative contributions of VEGF-B and PlGF to VEGFR-1 signaling may be masked in the presence of VEGF-A, which is abundantly expressed during postnatal development. To test this hypothesis, neonatal or adult mice were treated with a monoclonal antibody (G6-23-IgG) blocking murine VEGF-A or a soluble VEGFR-1 receptor IgG chimeric construct [mFlt(1-3)-IgG], which neutralizes VEGF-A, VEGF-B, and PlGF. Both compounds attenuated growth and survival of neonatal mice to similar extents and the pathophysiologic alterations, including a reduction in organ size and vascularization, changes in gene expression, and hematologic end points, were essentially indistinguishable. In adult mice, we observed only minor changes in response to treatment, which were similar between both anti-VEGF compounds. In conclusion, our findings suggest that PlGF and VEGF-B do not compensate during conditions of VEGF-A blockade, suggesting a minor role for compensatory VEGFR-1 signaling during postnatal development and vascular homeostasis in adults. The absence of compensatory VEGFR-1 signaling by VEGF-B and PlGF may have important implications for the development of anticancer strategies targeting the VEGF ligand/receptor system.
- Published
- 2006
- Full Text
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38. Racial differences in demographics, acute complications, and outcomes in patients with subarachnoid hemorrhage: a large patient series.
- Author
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Rosen D, Novakovic R, Goldenberg FD, Huo D, Baldwin ME, Frank JI, Rosengart AJ, and Macdonald RL
- Subjects
- Adult, Aged, Double-Blind Method, Female, Humans, Male, Middle Aged, Neuroprotective Agents therapeutic use, Patient Admission, Pregnatrienes therapeutic use, Randomized Controlled Trials as Topic, Retrospective Studies, Subarachnoid Hemorrhage complications, Subarachnoid Hemorrhage therapy, Treatment Outcome, Black or African American, Minority Groups, Subarachnoid Hemorrhage ethnology, White People
- Abstract
Object: Few studies have focused on the impact of racial differences in demographics, clinical characteristics, acute complications, and outcomes of patients with aneurysmal subarachnoid hemorrhage (SAH). The purpose of this study was to examine this issue., Methods: The authors evaluated prospectively collected data on 1711 adult patients with aneurysmal SAH who were entered into two randomized, double-blind, placebo-controlled trials conducted at neurosurgical centers in North America between 1991 and 1997. Admission characteristics, treatment modalities, in-hospital complications, and 3-month outcomes assessed by application of the Glasgow Outcome Scale were compared using the chi-square test, a t-test, the Wilcoxon rank-sum test, and multiple logistic regressions based on a significance level of 0.05 in 241 African-American, 1342 Caucasian, and 128 other racial minority patients. Caucasian patients were significantly older than patients of other races (p < 0.0001). African-American patients more frequently had a history of hypertension (p < 0.0001) and an elevated blood pressure at the time of admission (p < 0.0001). African-Americans and other racial minorities were more likely to have internal carotid artery aneurysms and Caucasians were more likely to have posterior circulation aneurysms (p = 0.0002). Rates of in-hospital complications were not significantly different except that pulmonary edema occurred more commonly in Caucasians (p = 0.036). After an adjustment was made for significant admission characteristics, the 3-month outcome was not significantly different among the races., Conclusions: Race was not found to be a prognostic factor for outcome after aneurysmal SAH. The higher SAH mortality rate previously observed in African-American patients is likely a result of a higher incidence of SAH in this group. These findings highlight the importance of primary prevention programs aimed at modifying risk factors for SAH.
- Published
- 2005
- Full Text
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39. Vascular endothelial growth factor D is dispensable for development of the lymphatic system.
- Author
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Baldwin ME, Halford MM, Roufail S, Williams RA, Hibbs ML, Grail D, Kubo H, Stacker SA, and Achen MG
- Subjects
- Animals, Endothelium, Lymphatic chemistry, Endothelium, Lymphatic metabolism, Gene Targeting, Lung chemistry, Lung cytology, Lung metabolism, Lymphangiogenesis physiology, Mice, Mice, Mutant Strains, Mutation genetics, Vascular Endothelial Growth Factor D genetics, Vascular Endothelial Growth Factor Receptor-3 analysis, Endothelium, Lymphatic cytology, Lymphangiogenesis genetics, Vascular Endothelial Growth Factor D physiology, Vascular Endothelial Growth Factor Receptor-3 physiology
- Abstract
Vascular endothelial growth factor receptor 3 (Vegfr-3) is a tyrosine kinase that is expressed on the lymphatic endothelium and that signals for the growth of the lymphatic vessels (lymphangiogenesis). Vegf-d, a secreted glycoprotein, is one of two known activating ligands for Vegfr-3, the other being Vegf-c. Vegf-d stimulates lymphangiogenesis in tissues and tumors; however, its role in embryonic development was previously unknown. Here we report the generation and analysis of mutant mice deficient for Vegf-d. Vegf-d-deficient mice were healthy and fertile, had normal body mass, and displayed no pathologic changes consistent with a defect in lymphatic function. The lungs, sites of strong Vegf-d gene expression during embryogenesis in wild-type mice, were normal in Vegf-d-deficient mice with respect to tissue mass and morphology, except that the abundance of the lymphatics adjacent to bronchioles was slightly reduced. Dye uptake experiments indicated that large lymphatics under the skin were present in normal locations and were functional. Smaller dermal lymphatics were similar in number, location, and function to those in wild-type controls. The lack of a profound lymphatic phenotype in Vegf-d-deficient mice suggests that Vegf-d does not play a major role in lymphatic development or that Vegf-c or another, as-yet-unknown activating Vegfr-3 ligand can compensate for Vegf-d during development.
- Published
- 2005
- Full Text
- View/download PDF
40. Early vasospasm on admission angiography in patients with aneurysmal subarachnoid hemorrhage is a predictor for in-hospital complications and poor outcome.
- Author
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Baldwin ME, Macdonald RL, Huo D, Novakovic RL, Goldenberg FD, Frank JI, and Rosengart AJ
- Subjects
- Adult, Aged, Cerebral Angiography, Female, Hospitalization, Humans, Male, Middle Aged, Prognosis, Subarachnoid Hemorrhage diagnostic imaging, Subarachnoid Hemorrhage physiopathology, Vasospasm, Intracranial diagnostic imaging, Vasospasm, Intracranial physiopathology
- Abstract
Background and Purpose: Early vasospasm (EVSP), defined here as arterial narrowing seen on diagnostic angiography within the first 48 hours of aneurysmal rupture, is a rarely reported and poorly defined phenomenon in patients with subarachnoid hemorrhage (SAH). The purpose of this study was to characterize EVSP in a large database of such patients., Methods: We analyzed the relationship of EVSP to clinical characteristics, in-hospital complications, and outcome at 3 months among 3478 patients entered into 4 prospective, randomized, double-blind, placebo-controlled trials of tirilazad conducted in neurosurgical centers around the world between 1991 and 1997., Results: Three hundred thirty-nine (10%) of 3478 patients had EVSP. EVSP was significantly more likely in patients with poor neurological grade on admission, history of SAH, intracerebral hematoma, larger aneurysm, thick SAH on cranial computed tomography, and intraventricular hemorrhage. EVSP was not associated with delayed cerebral vasospasm. After adjustment for differences in admission characteristics, EVSP was associated with cerebral infarction (adjusted odds ratios [OR]=1.51; 95% CI, 1.18 to 1.94; P=0.001), neurological worsening (OR=1.41; 95% CI, 1.10 to 1.81; P=0.007), and unfavorable outcome (OR=1.51; 95% CI, 1.15 to 2.00; P=0.003). In addition, there was a trend for patients with increasingly severe EVSP to have unfavorable outcome (OR=1.84 for mild and OR=2.66 for moderate/severe EVSP)., Conclusions: EVSP was seen in 10% of SAH patients and was predictive of cerebral infarction and neurological worsening as well as unfavorable outcome at 3 months. EVSP was not associated with late vasospasm. EVSP may be as important as delayed vasospasm in predicting complications and long-term morbidity in SAH patients.
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- 2004
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41. Expression of vascular endothelial growth factor receptor-3 by lymphatic endothelial cells is associated with lymph node metastasis in prostate cancer.
- Author
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Zeng Y, Opeskin K, Baldwin ME, Horvath LG, Achen MG, Stacker SA, Sutherland RL, and Williams ED
- Subjects
- Antibodies chemistry, Antibody Specificity, Blotting, Western, Cell Line, Humans, Immunohistochemistry, Immunoprecipitation, Lymphatic Metastasis, Male, Prostate metabolism, Protein Structure, Tertiary, Vascular Endothelial Growth Factor C metabolism, Vascular Endothelial Growth Factor D metabolism, Endothelial Cells metabolism, Lymph Nodes metabolism, Prostatic Neoplasms metabolism, Vascular Endothelial Growth Factor Receptor-3 biosynthesis
- Abstract
Purpose: The molecular mechanisms underlying lymph node metastasis are poorly understood, despite the well-established clinical importance of lymph node status in many human cancers. Recently, vascular endothelial growth factor (VEGF)-C and VEGF-D have been implicated in the regulation of tumor lymphangiogenesis and enhancement of lymphatic invasion via activation of VEGF receptor-3. The purpose of this study was to determine the expression pattern of the VEGF-C/VEGF-D/VEGF receptor-3 axis in prostate cancer and its relationship with lymph node metastasis., Experimental Design: The expression pattern of VEGF-C, VEGF-D, and VEGF receptor-3 in localized prostate cancer specimens (n = 37) was determined using immunohistochemistry., Results: Widespread, heterogeneous staining for VEGF-C and VEGF-D was observed in all cancer specimens. Intensity of VEGF-C staining was lower in benign prostate epithelium than in adjacent carcinoma, whereas no difference between benign epithelium and carcinoma was observed for VEGF-D staining. VEGF receptor-3 immunostaining was detected in endothelial cells of lymphatic vessels in 18 of 37 tissue samples. The presence of VEGF receptor-3-positive vessels was associated with lymph node metastasis (P = 0.0002), Gleason grade (P < 0.0001), extracapsular extension (P = 0.0382), and surgical margin status (P = 0.0069). In addition, VEGF receptor-3 staining highlighted lymphatic invasion by VEGF-C-positive/VEGF-D-positive carcinoma cells., Conclusions: Together, these results suggest that paracrine activation of lymphatic endothelial cell VEGF receptor-3 by VEGF-C and/or VEGF-D may be involved in lymphatic metastasis. Thus the VEGF-C/VEGF-D/VEGF receptor-3 signaling pathway may provide a target for antilymphangiogenic therapy in prostate cancer.
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- 2004
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42. Plasmin activates the lymphangiogenic growth factors VEGF-C and VEGF-D.
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McColl BK, Baldwin ME, Roufail S, Freeman C, Moritz RL, Simpson RJ, Alitalo K, Stacker SA, and Achen MG
- Subjects
- Animals, Endothelial Growth Factors genetics, Humans, Protein Isoforms genetics, Protein Isoforms metabolism, Recombinant Fusion Proteins metabolism, Vascular Endothelial Growth Factor C, Vascular Endothelial Growth Factor D, Vascular Endothelial Growth Factor Receptor-2 metabolism, Vascular Endothelial Growth Factor Receptor-3 metabolism, Endothelial Growth Factors metabolism, Fibrinolysin metabolism, Lymphatic System physiology, Neovascularization, Pathologic, Neovascularization, Physiologic
- Abstract
Vascular endothelial growth factor (VEGF) C and VEGF-D stimulate lymphangiogenesis and angiogenesis in tissues and tumors by activating the endothelial cell surface receptor tyrosine kinases VEGF receptor (VEGFR) 2 and VEGFR-3. These growth factors are secreted as full-length inactive forms consisting of NH2- and COOH-terminal propeptides and a central VEGF homology domain (VHD) containing receptor binding sites. Proteolytic cleavage removes the propeptides to generate mature forms, consisting of dimers of the VEGF homology domain, that bind receptors with much greater affinity than the full-length forms. Therefore, proteolytic processing activates VEGF-C and VEGF-D, although the proteases involved were unknown. Here, we report that the serine protease plasmin cleaved both propeptides from the VEGF homology domain of human VEGF-D and thereby generated a mature form exhibiting greatly enhanced binding and cross-linking of VEGFR-2 and VEGFR-3 in comparison to full-length material. Plasmin also activated VEGF-C. As lymphangiogenic growth factors promote the metastatic spread of cancer via the lymphatics, the proteolytic activation of these molecules represents a potential target for antimetastatic agents. Identification of an enzyme that activates the lymphangiogenic growth factors will facilitate development of inhibitors of metastasis.
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- 2003
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43. Regenerating lizard tails: a new model for investigating lymphangiogenesis.
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Daniels CB, Lewis BC, Tsopelas C, Munns SL, Orgeig S, Baldwin ME, Stacker SA, Achen MG, Chatterton BE, and Cooter RD
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- Animals, Blotting, Western, Endothelial Growth Factors analysis, Intercellular Signaling Peptides and Proteins analysis, Kinetics, Lizards anatomy & histology, Lymphatic System anatomy & histology, Lymphokines analysis, Tail, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factors, Lizards physiology, Lymphatic System physiology, Models, Animal, Regeneration
- Abstract
Impaired lymphatic drainage in human limbs causes the debilitating swelling termed lymphoedema. In mammals, known growth factors involved in the control of lymphangiogenesis (growth of new lymph vessels) are vascular endothelial growth factors-C and -D (VEGF-C/D). Here we characterize a model of lymphangiogenesis in which the tail of lizards is regenerated without becoming oedematous. Three weeks after the tail is shed (autotomy), there are a small number of large diameter lymphatic vessels in the regenerated tail. Thereafter, the number increases and the diameter decreases. A functional lymphatic network, as determined by lymphoscintigraphy, is established 6 wk after autotomy. The new network differs morphologically and functionally from that in original tails. This lymphatic regeneration is associated with an up-regulation of a reptilian homologue of the VEGF-C/D protein family (rVEGF-C/D), as determined by Western blot analysis using a human reactive VEGF-C polyclonal antibody. Regenerating lizard tails are potentially useful models for studying the molecular basis of lymphangiogenesis with a view to developing possible treatments for human lymphoedema.
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- 2003
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44. Molecular control of lymphangiogenesis.
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Baldwin ME, Stacker SA, and Achen MG
- Subjects
- Animals, Body Fluids metabolism, Homeostasis, Humans, Lymphatic System physiology, Lymphatic System physiopathology, Models, Biological, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factors, Endothelial Growth Factors metabolism, Intercellular Signaling Peptides and Proteins metabolism, Lymphatic System growth & development, Lymphokines metabolism, Receptors, Vascular Endothelial Growth Factor metabolism
- Abstract
The lymphatic vasculature plays a critical role in the regulation of body fluid volume and immune function. Extensive research into the molecular mechanisms that control blood vessel growth has led to identification of molecules that also regulate development and growth of the lymphatic vessels. This is generating a great deal of interest in the molecular control of the lymphatics in the context of embryogenesis, lymphatic disorders and tumor metastasis. Studies in animal models carried out over the past three years have shown that the soluble protein growth factors, vascular endothelial growth factor (VEGF)-C and VEGF-D, and their cognate receptor tyrosine kinase, VEGF receptor-3 (VEGFR-3), are critical regulators of lymphangiogenesis. Furthermore, disfunction of VEGFR-3 has recently been shown to cause lymphedema. The capacity to induce lymphangiogenesis by manipulation of the VEGF-C/VEGF-D/VEGFR-3 signaling pathway offers new opportunities to understand the function of the lymphatic system and to develop novel treatments for lymphatic disorders., (Copyright 2002 Wiley-Periodicals, Inc.)
- Published
- 2002
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45. Lymphangiogenesis and cancer metastasis.
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Stacker SA, Achen MG, Jussila L, Baldwin ME, and Alitalo K
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- Animals, Growth Substances metabolism, Humans, Lymphatic System growth & development, Lymphatic System metabolism, Signal Transduction, Vascular Endothelial Growth Factor D, Lymphatic Metastasis pathology, Lymphatic System pathology, Neoplasms pathology
- Abstract
Lymphatic vessels are important for the spread of solid tumours, but the mechanisms that underlie lymphatic spread and the role of lymphangiogenesis (the growth of lymphatics) in tumour metastasis has been less clear. This article reviews recent experimental and clinico-pathological data indicating that growth factors that stimulate lymphangiogenesis in tumours are associated with an enhanced metastatic process.
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- 2002
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46. The role of tumor lymphangiogenesis in metastatic spread.
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Stacker SA, Baldwin ME, and Achen MG
- Subjects
- Animals, Biomarkers analysis, Endothelial Growth Factors physiology, Endothelium chemistry, Humans, Lymphatic System anatomy & histology, Lymphatic System growth & development, Lymphatic System physiology, Lymphokines physiology, Models, Biological, Neoplasms etiology, Neoplasms therapy, Neovascularization, Pathologic, Vascular Endothelial Growth Factor A, Vascular Endothelial Growth Factors, Lymphatic Metastasis, Neoplasms pathology
- Abstract
The high mortality rates associated with cancer can be attributed to the metastatic spread of tumor cells from the site of their origin. Tumor cells invade either the blood or lymphatic vessels to access the general circulation and then establish themselves in other tissues. Clinicopathological data suggest that the lymphatics are an initial route for the spread of solid tumors. Detection of sentinel lymph nodes by biopsy provides significant information for staging and designing therapeutic regimens. The role of angiogenesis in facilitating the growth of solid tumors has been well established, but the presence of lymphatic vessels and the relevance of lymphangiogenesis to tumor spread are less clear. Recently, the molecular pathway that signals for lymphangiogenesis and relatively specific markers for lymphatic endothelium have been described allowing analyses of tumor lymphangiogenesis to be performed in animal models. These studies demonstrate that tumor lymphangiogenesis is a major component of the metastatic process and implicate members of the VEGF family of growth factors as key mediators of lymphangiogenesis in both normal biology and tumors.
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- 2002
- Full Text
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47. The angiogenic and lymphangiogenic factor vascular endothelial growth factor-D exhibits a paracrine mode of action in cancer.
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Achen MG, Williams RA, Baldwin ME, Lai P, Roufail S, Alitalo K, and Stacker SA
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- Animals, Blotting, Western, Breast Neoplasms metabolism, Carcinoma, Intraductal, Noninfiltrating metabolism, Carcinoma, Non-Small-Cell Lung metabolism, Endothelium, Vascular metabolism, Humans, Immunohistochemistry, In Situ Hybridization, Lung Neoplasms metabolism, Mice, Mice, SCID, Models, Biological, Neoplasm Metastasis, Neoplasm Transplantation, Precipitin Tests, RNA, Messenger metabolism, Tumor Cells, Cultured, Vascular Endothelial Growth Factor D, Vascular Endothelial Growth Factor Receptor-2 metabolism, Vascular Endothelial Growth Factor Receptor-3 metabolism, Endothelial Growth Factors metabolism, Lymph Nodes metabolism, Neoplasms metabolism, Neovascularization, Pathologic
- Abstract
Vascular endothelial growth factor-D (VEGF-D) promotes angiogenesis, lymphangiogenesis and metastatic spread via the lymphatics, however, the mode of VEGF-D action (e.g. paracrine vs. autocrine) was unknown. We analyzed VEGF-D action in human tumors and a mouse model of metastasis. VEGF-D was localized in tumor cells and endothelium in human non-small cell lung carcinoma and breast ductal carcinoma in situ. Tumor vessels positive for VEGF-D were also positive for its receptors, VEGF receptor-2 (VEGFR-2) and/or VEGFR-3 but negative for VEGF-D mRNA, indicating that VEGF-D is secreted by tumor cells and subsequently associates with endothelium via receptor-mediated uptake. The mature form of VEGF-D was detected in tumors demonstrating that VEGF-D is proteolytically processed and bioactive. In a mouse model of metastasis, VEGF-D synthesized in tumor cells became localized on the endothelium and thereby promoted metastatic spread. These data indicate that VEGF-D promotes tumor angiogenesis, lymphangiogenesis and metastatic spread by a paracrine mechanism.
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- 2002
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48. Multiple forms of mouse vascular endothelial growth factor-D are generated by RNA splicing and proteolysis.
- Author
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Baldwin ME, Roufail S, Halford MM, Alitalo K, Stacker SA, and Achen MG
- Subjects
- Amino Acid Sequence, Animals, Base Sequence, Endothelial Growth Factors chemistry, Endothelial Growth Factors metabolism, Glycosylation, Humans, Hydrolysis, Mice, Molecular Sequence Data, Protein Isoforms chemistry, Protein Isoforms metabolism, Reverse Transcriptase Polymerase Chain Reaction, Vascular Endothelial Growth Factor D, Endothelial Growth Factors genetics, Protein Isoforms genetics, RNA Splicing
- Abstract
The secreted glycoprotein vascular endothelial growth factor-D (VEGF-D) is angiogenic, lymphangiogenic, and promotes metastatic spread of tumor cells via lymphatic vessels. VEGF-D consists of a receptor-binding domain (VEGF homology domain) and N- and C-terminal propeptides. Proteolytic processing produces numerous forms of human VEGF-D, including fully processed derivatives (containing only the VEGF homology domain), partially processed, and unprocessed derivatives. Proteolysis is essential to generate human VEGF-D that binds the angiogenic receptor VEGF receptor-2 (VEGFR-2) and the lymphangiogenic receptor VEGFR-3 with high affinity. Here, we report that alternative use of an RNA splice donor site in exon 6 of the mouse VEGF-D gene produces two different protein isoforms, VEGF-D(358) and VEGF-D(326), with distinct C termini. The two isoforms were both expressed in all adult mouse tissues and embryonic stages of development analyzed. Both isoforms are proteolytically processed in a similar fashion to human VEGF-D to generate a range of secreted derivatives and bind and cross-link VEGFR-3 with similar potency. The isoforms are differently glycosylated when expressed in vitro. This study demonstrates that RNA splicing, protein glycosylation, and proteolysis are mechanisms for generating structural diversity of mouse VEGF-D.
- Published
- 2001
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49. The specificity of receptor binding by vascular endothelial growth factor-d is different in mouse and man.
- Author
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Baldwin ME, Catimel B, Nice EC, Roufail S, Hall NE, Stenvers KL, Karkkainen MJ, Alitalo K, Stacker SA, and Achen MG
- Subjects
- Amino Acid Sequence, Animals, Binding Sites, Biological Assay, Biosensing Techniques, Blotting, Western, Cross-Linking Reagents pharmacology, Electrophoresis, Polyacrylamide Gel, Embryo, Mammalian metabolism, Endothelial Growth Factors biosynthesis, Endothelium, Vascular metabolism, Epidermis metabolism, Humans, Immunohistochemistry, In Situ Hybridization, Kinetics, Ligands, Mice, Models, Molecular, Molecular Sequence Data, Mutation, Protein Binding, Protein Conformation, Protein Structure, Tertiary, Receptor Protein-Tyrosine Kinases metabolism, Receptors, Growth Factor metabolism, Receptors, Vascular Endothelial Growth Factor, Sequence Homology, Amino Acid, Skin embryology, Skin metabolism, Time Factors, Vascular Endothelial Growth Factor D, Vascular Endothelial Growth Factor Receptor-3, Endothelial Growth Factors metabolism
- Abstract
Human vascular endothelial growth factor-D (VEGF-D) binds and activates VEGFR-2 and VEGFR-3, receptors expressed on vascular and lymphatic endothelial cells. As VEGFR-2 signals for angiogenesis and VEGFR-3 is thought to signal for lymphangiogenesis, it was proposed that VEGF-D stimulates growth of blood vessels and lymphatic vessels into regions of embryos and tumors. Here we report the unexpected finding that mouse VEGF-D fails to bind mouse VEGFR-2 but binds and cross-links VEGFR-3 as demonstrated by biosensor analysis with immobilized receptor domains and bioassays of VEGFR-2 and VEGFR-3 cross-linking. Mutation of amino acids in mouse VEGF-D to those in the human homologue indicated that residues important for the VEGFR-2 interaction are clustered at, or are near, the predicted receptor-binding surface. Coordinated expression of VEGF-D and VEGFR-3 in mouse embryos was detected in the developing skin where the VEGF-D gene was expressed in a layer of cells beneath the developing epidermis and VEGFR-3 was localized on a network of vessels immediately beneath the VEGF-D-positive cells. This suggests that VEGF-D and VEGFR-3 may play a role in establishing vessels of the skin by a paracrine mechanism. Our study of receptor specificity suggests that VEGF-D may have different biological functions in mouse and man.
- Published
- 2001
- Full Text
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50. VEGF-D promotes the metastatic spread of tumor cells via the lymphatics.
- Author
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Stacker SA, Caesar C, Baldwin ME, Thornton GE, Williams RA, Prevo R, Jackson DG, Nishikawa S, Kubo H, and Achen MG
- Subjects
- Animals, Cell Line, Transformed, Endothelial Growth Factors genetics, Endothelial Growth Factors metabolism, Female, Humans, Lymphatic Metastasis, Mice, Mice, Inbred NOD, Mice, SCID, Neoplasms pathology, Neoplasms physiopathology, Vascular Endothelial Growth Factor D, Endothelial Growth Factors physiology, Neovascularization, Pathologic
- Abstract
Metastasis to local lymph nodes via the lymphatic vessels is a common step in the spread of solid tumors. To investigate the molecular mechanisms underlying the spread of cancer by the lymphatics, we examined the ability of vascular endothelial growth factor (VEGF)-D, a ligand for the lymphatic growth factor receptor VEGFR-3/Flt-4, to induce formation of lymphatics in a mouse tumor model. Staining with markers specific for lymphatic endothelium demonstrated that VEGF-D induced the formation of lymphatics within tumors. Moreover, expression of VEGF-D in tumor cells led to spread of the tumor to lymph nodes, whereas expression of VEGF, an angiogenic growth factor which activates VEGFR-2 but not VEGFR-3, did not. VEGF-D also promoted tumor angiogenesis and growth. Lymphatic spread induced by VEGF-D could be blocked with an antibody specific for VEGF-D. This study demonstrates that lymphatics can be established in solid tumors and implicates VEGF family members in determining the route of metastatic spread.
- Published
- 2001
- Full Text
- View/download PDF
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